Variant #0000000069 (NC_000013.10:g.32911300_32911303del, NM_000059.3:c.2808_2811del (BRCA2))

Chromosome 13
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.32911300_32911303del
Reference -
DB-ID BRCA2_000017
Frequency -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2019-02-21 11:05:57 +00:00 (UTC)
Date last edited 2023-06-27 13:21:08 +00:00 (UTC)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BRCA2 NM_000059.3 +/+ 11 c.2808_2811del r.(?) p.(Ala938Profs*21)